🔍 RecallPedia

Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Class I - Dangerous
Recalled: August 8, 2016 Pharmatech Supplements

What Should You Do?

  1. Check if you have this product:
    NDC No. 0904-6060-50; Lot No. 20901509 & 20901510, Exp. Date 11/2017; Lot No. 20901601, Exp. Date 02/2018; Lot No. 20901602, Exp. Date 03/2018; Lot No. 20901603, Exp. Date 05/2018.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Pharmatech LLC
Reason for Recall:
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement.

Product Codes/Lot Numbers:

NDC No. 0904-6060-50; Lot No. 20901509 & 20901510, Exp. Date 11/2017; Lot No. 20901601, Exp. Date 02/2018; Lot No. 20901602, Exp. Date 03/2018; Lot No. 20901603, Exp. Date 05/2018.

Distribution:

Distributed in: FL, MI, MS, OH

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0269-2017

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